Literature DB >> 25483011

Safety of off-label biologicals in systemic lupus erythematosus.

Martin Aringer1, Josef S Smolen.   

Abstract

INTRODUCTION: The approval of belimumab and other advances in the field have narrowed the window for off-label use of biologicals in systemic lupus erythematosus (SLE). For consideration in severe and refractory disease, safety will play a major role. AREAS COVERED: We reviewed the literature on safety aspects of off-label biological use in SLE. Significant evidence is available for rituximab, whereas data on the off-label SLE therapy with other biologicals are much more limited. Published trials and open-label experience in SLE allow for some conclusions on abatacept, and on approaches targeting TNF, IL-1 and IL-6 receptors. EXPERT OPINION: Anti-TNF antibodies apparently are the only ones inducing SLE-specific autoantibodies, but even these were not associated with flares. Risks for severe infections certainly remain a major serious concern, particularly in combinations with glucocorticoids and/or immunosuppressants. These findings reiterate that experience with both the disease and the drugs will be essential for keeping patients safe. The available data suggest a manageable adverse event profile for rituximab and do not prove unacceptable risks for other biologicals. Reports frequently only include very few patients, with the inherent danger of bias due to lacking reports on failed treatment attempts.

Entities:  

Keywords:  abatacept; adverse events; etanercept; infections; infliximab; malignancy; progressive multifocal leukoencephalopathy; rituximab; sle; tocilizumab

Mesh:

Substances:

Year:  2014        PMID: 25483011     DOI: 10.1517/14740338.2015.986455

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  3 in total

Review 1.  Beyond pan-B-cell-directed therapy - new avenues and insights into the pathogenesis of SLE.

Authors:  Thomas Dörner; Peter E Lipsky
Journal:  Nat Rev Rheumatol       Date:  2016-10-13       Impact factor: 20.543

2.  Methyl salicylate 2-O-β-d-lactoside alleviates the pathological progression of pristane-induced systemic lupus erythematosus-like disease in mice via suppression of inflammatory response and signal transduction.

Authors:  Yang-Yang He; Yu Yan; Hui-Fang Zhang; Yi-Huang Lin; Yu-Cai Chen; Yi Yan; Ping Wu; Jian-Song Fang; Shu-Hui Yang; Guan-Hua Du
Journal:  Drug Des Devel Ther       Date:  2016-09-29       Impact factor: 4.162

3.  JAK inhibitor has the amelioration effect in lupus-prone mice: the involvement of IFN signature gene downregulation.

Authors:  Keigo Ikeda; Kunihiro Hayakawa; Maki Fujishiro; Mikiko Kawasaki; Takuya Hirai; Hiroshi Tsushima; Tomoko Miyashita; Satoshi Suzuki; Shinji Morimoto; Naoto Tamura; Kenji Takamori; Hideoki Ogawa; Iwao Sekigawa
Journal:  BMC Immunol       Date:  2017-08-22       Impact factor: 3.615

  3 in total

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